Hydrochloric Acid → HCID 178494697, compound

Sodium methylate (11.90 g, 0.22 mole) was added to a solution of methoxyacetamidine hydrochloride (12.45 g, 0.1 mole) and ethyl 4-chloroacetoacetate (16.50 g, 0.1 mole) in methanol (50 ml) at 5° to 10° C. with stirring. The resulting orange reaction mixture was stirred at 5° to 10° C. for 2 hours and then at 20° C. for 3 hours, and neutralized with conc. hydrochloric acid. The precipitate was filtered, and the filtrate was concentrated under reduced pressure to obtain a residue which was then dissolved in water (300 ml). The aqueous solution was extracted with chloroform, and the chloroform extract was dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain a crystalline residue. The residue was suspended in ether and then filtered to obtain 17.8 g of 6-(chloromethyl)-4-hydroxy-2-(methoxymethyl)pyrimidine as pale brown needle-like crystals (m.p. 124.0°-125.5° C.).

1. stirringThe resulting orange reaction mixture was stirred at 5° to 10° C. for 2 hours
2. filtrationThe precipitate was filtered
3. concentrationthe filtrate was concentrated under reduced pressure
4. customto obtain a residue which
5. extractionThe aqueous solution was extracted with chloroform
6. extractionthe chloroform extract
7. dry with materialwas dried over anhydrous sodium sulfate
8. concentrationconcentrated under reduced pressure
9. customto obtain a crystalline residue
10. filtrationfiltered

ORD record

ord-76ee4867c34f429aa7411b119e3786ef

Source dataset

uspto-grants-1981_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04308258